Onsite Seattle preferred but will consider remote for ideal candidate
W2 Only – 6 month contract
Responsible for statistical aspects of clinical and pre-clinical research projects including study design, sample size estimation, patient randomization, case report form development, writing statistical analysis plans, statistical analysis and interpretation of data, and reporting of results. Work with SAS programmers as part of a biostatistics team.
Knowledge of applied parametric and nonparametric statistics, strong SAS programming skills, and the ability to translate client needs into statistical practice and the ability to educate clients in the use of statistics are essential.
Excellent verbal and written communication skills.
Candidate with 2+ years experience conducting statistical analysis of clinical research data.
Experience using SAS, Oracle Clinical, and/or ClinTrial.
Typically has a Masters or a Ph.D. degree in statistics, biostatistics, or related field with at least 6 years of pharmaceutical or related experience.